Evaluation of Pulpotomy, Partial Pulpotomy, and Direct Pulp Capping Using Mineral Trioxide Aggregate.

NCT ID: NCT07333872

Last Updated: 2026-01-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

96 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-01

Study Completion Date

2026-06-20

Brief Summary

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A comparative evaluation for three vital pulp therapy techniques in primary molars using the same material (MTA)

Detailed Description

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Conditions

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Vital Pulp Therapy in Primary Teeth

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Direct pulp capping

Technique of vital pulp therapy to cap pin point exposure

Group Type EXPERIMENTAL

pulp capping with MTA

Intervention Type PROCEDURE

Capping of the pulp tissue with a biocompatible material (MTA)

Partial pulpotomy

Technique of vital pulp therapy to cap widened pulp exposure

Group Type EXPERIMENTAL

pulp capping with MTA

Intervention Type PROCEDURE

Capping of the pulp tissue with a biocompatible material (MTA)

Pulpotomy

Technique of vital pulp therapy of capping radicular pulp after removal of coronal pulp

Group Type EXPERIMENTAL

pulp capping with MTA

Intervention Type PROCEDURE

Capping of the pulp tissue with a biocompatible material (MTA)

Interventions

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pulp capping with MTA

Capping of the pulp tissue with a biocompatible material (MTA)

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* articipants were cooperative children (4-7 years) with no systemic diseases or relevant allergies. Eligible teeth were restorable primary second molars with deep carious lesions and a diagnosis of reversible pulpitis,

Exclusion Criteria

* spontaneous pain, edema, fistula, pathological mobility, or percussion sensitivity.
Minimum Eligible Age

4 Years

Maximum Eligible Age

7 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Delta University for Science and Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Delta university for science and technology

Gamasa, Dakahlia Governorate, Egypt

Site Status

Countries

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Egypt

Other Identifiers

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DU:025052113

Identifier Type: -

Identifier Source: org_study_id

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